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  2. Informed consent - Wikipedia

    en.wikipedia.org/wiki/Informed_consent

    The informed consent doctrine is generally implemented through good healthcare practice: pre-operation discussions with patients and the use of medical consent forms in hospitals. However, reliance on a signed form should not undermine the basis of the doctrine in giving the patient an opportunity to weigh and respond to the risk.

  3. Dynamic consent - Wikipedia

    en.wikipedia.org/wiki/Dynamic_consent

    Dynamic consent is an approach to informed consent that enables on-going engagement and communication between individuals and the users and custodians of their data. It is designed to address the many issues that are raised by the use of digital technologies in research and clinical care that enable the wide-scale use, linkage, analysis and integration of diverse datasets and the use of AI and ...

  4. Case report form - Wikipedia

    en.wikipedia.org/wiki/Case_report_form

    Examples of data that would lead to a query: a male patient being on female birth control medication or having had an abortion, or a 15-year-old participant having had hip replacement surgery. Each query has to be resolved by the individual attention of a member of each local research team, as well as an individual in the study administration.

  5. Informed assent - Wikipedia

    en.wikipedia.org/wiki/Informed_assent

    According to CESP, child-focused forms should include all the elements and considerations generally required for seeking informed consent of competent adults. [7] Additionally, it should conform to their intellectual capacity to understand the reason for the research and the risks therein, and the family should be given sufficient time and ...

  6. Institutional review board - Wikipedia

    en.wikipedia.org/wiki/Institutional_review_board

    An institutional review board (IRB), also known as an independent ethics committee (IEC), ethical review board (ERB), or research ethics board (REB), is a committee at an institution that applies research ethics by reviewing the methods proposed for research involving human subjects, to ensure that the projects are ethical.

  7. Experiment - Wikipedia

    en.wikipedia.org/wiki/Experiment

    By placing the distribution of the independent variable(s) under the control of the researcher, an experiment—particularly when it involves human subjects—introduces potential ethical considerations, such as balancing benefit and harm, fairly distributing interventions (e.g., treatments for a disease), and informed consent. For example, in ...

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